Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_assertion description "[Recent studies in four kindreds showed linkage of a gene for FJHN to the same genomic interval on chromosome 16p11.2, where the gene for the phenotypically similar medullary cystic disease type 2 (MCKD2) has been localised.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_assertion evidence source_evidence_literature NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_assertion SIO_000772 12634862 NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_assertion wasDerivedFrom befree-20140225 NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_assertion wasGeneratedBy ECO_0000203 NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP551948.RATRbSvykmonO5zEc0_EQGdZVnN_lgpGK0geqNDCv2JKE130_provenance.